SerpinB3 administration protects liver against ischemia-reperfusion injury

We have investigated the change in SerpinB3 during hepatic ischemia and the potential role of its antiprotease activity in cell protection by the administration of wild-type SerpinB3 (SerpinB3-WT) or active loop-deleted recombinant SerpinB3 protein (SerpinB3-D) in a rat model of ischemia (60 min)/r...

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Main Authors: Cristian Turato, Mariapia Vairetti, Marta Cagna, Alessandra Biasiolo, Andrea Ferrigno, Santina Quarta, Mariagrazia Ruvoletto, Silvia De Siervi, Patrizia Pontisso, Laura Giuseppina Di Pasqua
Format: Article
Language:English
Published: PAGEPress Publications 2022-10-01
Series:European Journal of Histochemistry
Subjects:
Online Access:https://www.ejh.it/index.php/ejh/article/view/3561
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author Cristian Turato
Mariapia Vairetti
Marta Cagna
Alessandra Biasiolo
Andrea Ferrigno
Santina Quarta
Mariagrazia Ruvoletto
Silvia De Siervi
Patrizia Pontisso
Laura Giuseppina Di Pasqua
author_facet Cristian Turato
Mariapia Vairetti
Marta Cagna
Alessandra Biasiolo
Andrea Ferrigno
Santina Quarta
Mariagrazia Ruvoletto
Silvia De Siervi
Patrizia Pontisso
Laura Giuseppina Di Pasqua
author_sort Cristian Turato
collection DOAJ
description We have investigated the change in SerpinB3 during hepatic ischemia and the potential role of its antiprotease activity in cell protection by the administration of wild-type SerpinB3 (SerpinB3-WT) or active loop-deleted recombinant SerpinB3 protein (SerpinB3-D) in a rat model of ischemia (60 min)/reperfusion (60 min) (I/R). A time-dependent increase of SerpinB3, both at transcription and protein level, was found in ischemic livers after 60, 120 and 180 min. SerpinB3-WT decreased polymorphonuclear cell infiltration and serum enzymes and increased ATP when compared with I/R group. These events were not obtained using SerpinB3-D. No significant changes in both liver SerpinB3 mRNA and protein were found in all I/R groups considered. The present data show that the administration of SerpinB3-WT reduced the I/R injury and this effect appears to be dependent on its anti-protease activity.  
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spelling doaj.art-132dd393be9445019719bfe2e49b6ede2022-12-22T03:54:10ZengPAGEPress PublicationsEuropean Journal of Histochemistry1121-760X2038-83062022-10-0166410.4081/ejh.2022.3561SerpinB3 administration protects liver against ischemia-reperfusion injuryCristian Turato0Mariapia Vairetti1Marta Cagna2Alessandra Biasiolo3Andrea Ferrigno4Santina Quarta5Mariagrazia Ruvoletto6Silvia De Siervi7Patrizia Pontisso8Laura Giuseppina Di Pasqua9Department of Molecular Medicine, University of PaviaDepartmentt of Internal Medicine and Therapeutics, University of PaviaDepartment of Internal Medicine and Therapeutics, University of PaviaDepartment of Medicine, University of Padua; LifeLab Program, Consorzio per la Ricerca Sanitaria (CORIS), Veneto Region, PaduaDepartment of Internal Medicine and Therapeutics, University of PaviaDepartment of Medicine, University of Padua; LifeLab Program, Consorzio per la Ricerca Sanitaria (CORIS), Veneto Region, PaduaDepartment of Medicine, University of Padua; LifeLab Program, Consorzio per la Ricerca Sanitaria (CORIS), Veneto Region, PaduaDepartment of Molecular Medicine, University of PaviaDepartment of Medicine, University of Padua; LifeLab Program, Consorzio per la Ricerca Sanitaria (CORIS), Veneto Region, PaduaDepartment of Internal Medicine and Therapeutics, University of Pavia We have investigated the change in SerpinB3 during hepatic ischemia and the potential role of its antiprotease activity in cell protection by the administration of wild-type SerpinB3 (SerpinB3-WT) or active loop-deleted recombinant SerpinB3 protein (SerpinB3-D) in a rat model of ischemia (60 min)/reperfusion (60 min) (I/R). A time-dependent increase of SerpinB3, both at transcription and protein level, was found in ischemic livers after 60, 120 and 180 min. SerpinB3-WT decreased polymorphonuclear cell infiltration and serum enzymes and increased ATP when compared with I/R group. These events were not obtained using SerpinB3-D. No significant changes in both liver SerpinB3 mRNA and protein were found in all I/R groups considered. The present data show that the administration of SerpinB3-WT reduced the I/R injury and this effect appears to be dependent on its anti-protease activity.   https://www.ejh.it/index.php/ejh/article/view/3561Ischemia/reperfusionSerpinB3inflammation
spellingShingle Cristian Turato
Mariapia Vairetti
Marta Cagna
Alessandra Biasiolo
Andrea Ferrigno
Santina Quarta
Mariagrazia Ruvoletto
Silvia De Siervi
Patrizia Pontisso
Laura Giuseppina Di Pasqua
SerpinB3 administration protects liver against ischemia-reperfusion injury
European Journal of Histochemistry
Ischemia/reperfusion
SerpinB3
inflammation
title SerpinB3 administration protects liver against ischemia-reperfusion injury
title_full SerpinB3 administration protects liver against ischemia-reperfusion injury
title_fullStr SerpinB3 administration protects liver against ischemia-reperfusion injury
title_full_unstemmed SerpinB3 administration protects liver against ischemia-reperfusion injury
title_short SerpinB3 administration protects liver against ischemia-reperfusion injury
title_sort serpinb3 administration protects liver against ischemia reperfusion injury
topic Ischemia/reperfusion
SerpinB3
inflammation
url https://www.ejh.it/index.php/ejh/article/view/3561
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AT mariapiavairetti serpinb3administrationprotectsliveragainstischemiareperfusioninjury
AT martacagna serpinb3administrationprotectsliveragainstischemiareperfusioninjury
AT alessandrabiasiolo serpinb3administrationprotectsliveragainstischemiareperfusioninjury
AT andreaferrigno serpinb3administrationprotectsliveragainstischemiareperfusioninjury
AT santinaquarta serpinb3administrationprotectsliveragainstischemiareperfusioninjury
AT mariagraziaruvoletto serpinb3administrationprotectsliveragainstischemiareperfusioninjury
AT silviadesiervi serpinb3administrationprotectsliveragainstischemiareperfusioninjury
AT patriziapontisso serpinb3administrationprotectsliveragainstischemiareperfusioninjury
AT lauragiuseppinadipasqua serpinb3administrationprotectsliveragainstischemiareperfusioninjury